4.8 Article

Aqueous Two-Phase System (ATPS)-Based Polymersomes for Particle Isolation and Separation

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 49, 页码 55467-55475

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c16968

关键词

aqueous two-phase system (ATPS); microfluidics; polymersome; isolation; separation

资金

  1. National Research Foundation of Korea (NRF) - Korean Government (MSIT) [NRF-2020R1C1C1004642]
  2. Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HP20C0006]
  3. National Research Foundation of Korea [4120200413631] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Aqueous two-phase systems (ATPSs) have been widely used in the separation, purification, and enrichment of biomolecules for their excellent biocompatibility. While ultra-centrifugation and microfluidic devices have been combined with ATPS to facilitate the separation of biomolecules and achieve high recovery yields, they often lack the ability to effectively isolate and separate biomolecules in low concentrations. In this work, we present a strategy that leverages the preferential partitioning of biomolecules in ATPS droplets to efficiently separate model extracellular vesicle (EV) particles. We demonstrate that the additional oil phase between the inner ATPS droplets and the aqueous continuous phase in triple emulsion droplets resolves the size controllability and instability issues of ATPS droplets, enabling the production of highly monodisperse ATPS-based polymersomes with enhanced stability for effective isolation of ATPS droplets from the surrounding environment. Furthermore, we achieve separation of model EV particles in a single dextran (DEX)-rich droplet by the massive production of ATPS-based polymersomes and osmotic-pressure-induced rupture of the selected polymersome in a hypertonic solution composed of poly(ethylene glycol) (PEG).

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